Details of SAPdb ID 1357 |
Primary information | ||
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SAPdb_ID | 1357 | |
PMID | 24036697 | |
Year | 2013 | |
Name | CDP or H–Phe–Phe–NH2. HCl | |
Sequence | FF | |
N-Terminal Modification | Free | |
C-Terminal Modification | Amidation | |
Non-terminal Modication | None | |
Length | 2 | |
Peptide/Conjugate/Mixture | Peptide | |
Conjugate Partner | Co-assemble with MO (Methyl orange) | |
Technique | Scanning Electron Microscopy (SEM) | |
Solvent | HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water | |
Method | Peptide added to water and to dissolve peptide in solutioh 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) added. Upon adding aqueous solutions of azobenzenes i.e . CPABS to HFIP solution of CDP (in a 1 : 1 mole ratio) at room temperature, yellow precipitates formed rapidly, indicating generation of co-assembled nanostructures. | |
Concentration | NA | |
pH | NA | |
Temperature | Room temperature | |
Incubation Period | Several hours | |
Self-Assembly Formation | Yes | |
Type of Self-Assembly | Plate like Nanostructure | |
Size of Self-Assembled structure | Diameter: 2μm, width: 1μm | |
Linear/Cyclic | Linear | |
Stability of Nanostructure | NA | |
Comment | NA | |
Secondary information | ||
Physico-Chemical properties |
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STRUCTURE |
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SMILES | N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N |